灵敏度(控制系统)
激发波长
发光
光电子学
材料科学
兴奋剂
波长
激发
卤化物
传输(电信)
锡
化学
电信
物理
无机化学
计算机科学
电子工程
量子力学
工程类
冶金
作者
Jianglong Chang,Sai Xu,Yuefeng Gao,You Li,Yichao Wang,Hongquan Yu,Yongze Cao,Xizhen Zhang,Baojiu Chen
标识
DOI:10.1002/admt.202401672
摘要
Abstract The coordination structure of Sb 3+ within the host lattice critically influences its photophysical properties, sparking interest in luminescent metal halides with multiexciton emissions. Furthermore, the multi‐coordination lattice structure of Sb 3+ dynamically emits light with excitation wavelength, highlighting the potential of Sb 3+ ions in tuning luminescence and developing advanced optoelectronic materials. Herein, Sb 3+ ions are successfully doped into Cs 2 SnCl 6 , and the obvious excitation wavelength‐dependent emission of Cs 2 SnCl 6 : Sb at room temperature is observed. To explain this phenomenon, density functional theory (DFT) calculations and time‐resolved spectra are conducted to confirm that the emission originated from two luminescence centers associated with the [SbCl 6 ] 3− and [SbCl 5 ] 2− coordination. Based on the tunable emission of Cs 2 SnCl 6 : Sb and the effective electron transfer between two triplet self‐trapped exciton states induced by Bi 3+ and Sb 3+ , a pixelated code for information encryption is designed. The encoded patterns exhibit color changes under different UV wavelengths, enabling secure and straightforward information encryption. Furthermore, a sensitive UV wavelength sensor is prepared based on Cs 2 SnCl 6 : Bi/Sb, exploiting the monotonic relationship between chromaticity coordinates and wavelength, achieving a resolution superior to previously reported wavelength sensors. This study marks a substantial step toward advancing the multifunctional application of lead‐free metal halides.
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